NCT05913167

Brief Summary

Nephrectomy pain was higher. erector spina plan block and transversus abdominis plan block had shown to be effective in abdominal surgeries. This study aimed to compare these two bloc analgesic efficacy in laparoscopic nephrectomy patients. The primary aim is postoperative morphine consumption.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Aug 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress96%
Aug 2023Jun 2026

First Submitted

Initial submission to the registry

June 12, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

June 22, 2023

Completed
2 months until next milestone

Study Start

First participant enrolled

August 15, 2023

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2026

Last Updated

October 15, 2024

Status Verified

December 1, 2023

Enrollment Period

2.8 years

First QC Date

June 12, 2023

Last Update Submit

October 11, 2024

Conditions

Keywords

laparoscopynephrectomyerector spina plan blocktransversus abdominis plan blockmorphine consumptionanalgesia

Outcome Measures

Primary Outcomes (1)

  • Postoperative morphine consumption

    morphine patient controlled analgesia was applied to the patients

    24 hour postoperatively

Secondary Outcomes (2)

  • Peroperative remifentanil consumptions

    peroperatively

  • postoperative analgesia numeric rating scales

    postoperative 24 hours

Study Arms (2)

Erector spina plan block

ACTIVE COMPARATOR

Erector spina plan block will be administered to the patients in this group.

Procedure: laparoscopic nephrectomy

Transversus abdominis plan block

ACTIVE COMPARATOR

Transversus abdominis plan block will be administered to the patients in this group.

Procedure: laparoscopic nephrectomy

Interventions

laparoscopic nephrectomy

Erector spina plan blockTransversus abdominis plan block

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • age
  • patients undergoing laparoscopic nephrectomy
  • ASA 1-3

You may not qualify if:

  • \<18- \>65 \< age
  • patients undergoing open nephrectomy
  • ASA 4-5

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kocaeli University

Kocaeli, 41900, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Agnosia

Condition Hierarchy (Ancestors)

Perceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
Participants will not know which block was administered outcome assessors will not know which block was administered
Purpose
DIAGNOSTIC
Intervention Model
CROSSOVER
Model Details: erector spina and transversus abdominis plane blocks
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

June 12, 2023

First Posted

June 22, 2023

Study Start

August 15, 2023

Primary Completion (Estimated)

June 15, 2026

Study Completion (Estimated)

June 15, 2026

Last Updated

October 15, 2024

Record last verified: 2023-12

Data Sharing

IPD Sharing
Will not share

Locations